In the crystal structures of the title compounds, C(12)H(12)N(4)(2+).2BF(4)-, (I), and C(12)H(11)N(4)+.ClO(4)-, (II), respectively, infinite two- and one-dimensional architectures are built up via N-H...F [in (I)] and conventional N-H...N [in (II)] hydrogen bonding. The N-N single bond in (I) lies on a crystallographic centre of symmetry; as a result, the two pyridinium rings are parallel. In (II), the pyridinium and pyridyl ring planes are inclined with a dihedral angle of 14.45 (3) degrees.
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http://dx.doi.org/10.1107/S0108270107015764 | DOI Listing |
Acta Crystallogr E Crystallogr Commun
April 2024
Department of Chemistry and Biochemistry, Miami University, 651 E. High St., Oxford, Ohio 45056, USA.
The title compound, [Co(CHN)(CHN)](BF), is a five-coordinate Co complex based on the neutral ligands tris-[(1-benzyl-triazol-4-yl)meth-yl]amine (tbta) and imidazole. It exhibits a distorted trigonal bipyramidal geometry in which the equatorial positions are occupied by the three N-atom donors from the triazole rings of the tripodal tbta ligand. The apical amine N-atom donor of tbta and the N-atom donor of the imidazole ligand occupy the axial positions of the coordination sphere.
View Article and Find Full Text PDFActa Crystallogr E Crystallogr Commun
December 2020
Research Institute for Interdisciplinary Science, Okayama University, Okayama, 700-8530, Japan.
The crystal structures of the complexes (-4-2)--bis-[8-(di-methyl-phosphan-yl)quinoline-κ ,]nickel(II) bis-(perchlorate) nitro-methane monosolvate, [Ni(CHNP)](ClO)·CHNO (), and (-4-2)--bis-[8-(di-methyl-phos-phan-yl)quinoline-κ ,]platinum(II) bis-(tetra-fluoro-borate) aceto-nitrile monosolvate, [Pt(CHNP)](BF)·CHN (), are reported. In both complex cations, two phosphanyl-quinolines act as bidentate -donating chelate ligands and form the mutually configuration in the square-planar coordination geometry. The strong influence of the di-methyl-phosphanyl donor group is confirmed by the Ni-N bond lengths in , 1.
View Article and Find Full Text PDFChem Asian J
March 2020
Department of Chemistry and Chemical Biology, Indiana University Purdue University Indianapolis, Indianapolis, Indiana, 46202, USA.
Selectfluor, [1-chloromethyl-4-fluoro-1,4-diazoniabicyclo-[2.2.2]octane bis(tetrafluoroborate)], is not only an important electrophilic fluorinating agent but also a facile and efficient "fluorine-free" functional reagent in other organic reactions.
View Article and Find Full Text PDFJ Mol Model
February 2020
Departments of Physics & Key Laboratory of Photonic and Optical Detection in Civil Aviation, Civil Aviation Flight University of China, Guanghan, 618307, China.
Viologen-based ionic liquids can form various microscopic structures at different temperatures. In this work, the dynamics of dimethyl-viologen bis-(tetrafluoroborate) ([VIO][TfN]) ionic liquid within 400-800 K has been exploited by molecular dynamics simulations. [VIO][TfN] exhibits a supercooled liquid analogous diffusion and structural relaxation even at temperature T = 400 K, and behaves more like simple liquids as temperature increases.
View Article and Find Full Text PDFAcc Chem Res
February 2020
Department of Chemical Science and Engineering , Tokyo Institute of Technology, Nagatsuta , Yokohama 226-8502 , Japan.
Organofluorine compounds are key materials applied in daily life because of their versatile utility as functional materials, pharmaceuticals, and agrochemicals. Development of the selective fluorination of organic molecules under safe conditions is therefore one of the most important subjects in modern synthetic organofluorine chemistry. Thus, various electrophilic fluorination reagents such as XeF, (PhSO)NF (NFSI), EtNSF (DAST), (MeOCHCH)NSF (Deoxofluor), 1-chloromethyl-4-fluoro-1,4-diazoniabicyclo-[2.
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